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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615273Generated: November 2, 2026

Piperidine → HCID 69811336, compound

https://huagongshe.com/reaction/1615273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantOxindoleHCID 321710—
ReactantHCID 86651957HCID 86651957—
SolventMethanolHCID 887—
ProductHCID 69811336HCID 6981133679.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of (E)-3-(2-(pyridin-4-yl)vinyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazole-6-carbaldehyde (927 mg, 2.44 mmol), oxindole (325 mg, 2.44 mmol) and MeOH (20 mL) was added piperidine (24 uL, 0.244 mmol) and the reaction heated to 60° C. for 4 hours. A yellow precipitate crashed out of the reaction medium which was filtered and washed with MeOH to give the title compound (960 mg, 79%) as a yellow solid. MS ESI 495.3 [M+H]+, calcd for [C29H30N4O2Si+H]+ 495.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765748B2
Source datasetuspto-grants-2014_07
ORD IDord-e58a503efd9049c38bd5a258fbe4580d
Source noteuspto-grants-2014_07